Linked Life Data

19346670

Source:http://linkedlifedata.com/resource/pubmed/id/19346670

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2009-4-17
pubmed:abstractText
To elucidate the mechanism of action of prostaglandin I(2) (PGI(2)) and carbaprostacyclin, we studied their effect on DNA synthesis and proliferation in primary cultures of adult rat hepatocytes. Hepatocyte parenchymal cells, maintained in a serum-free, defined medium, synthesized DNA and proliferated in the presence of PGI(2) or carbaprostacyclin in a time- and dose-dependent manner. PGI(2) was less potent than carbaprostacyclin in stimulating hepatocyte mitogenesis. These effects of PGI(2) and carbaprostacyclin were abolished by treatment with a specific IP-receptor antagonist, CAY10441 (10(-9) - 10(-7) M). Hepatocyte mitogenesis induced by the IP-receptor agonists was almost completely blocked by specific inhibitors of growth-related signal transducers such as AG1478 (5 x 10(-7) M), LY294002 (10(-7) M), PD98059 (10(-6) M), and rapamycin (10 ng/ml). In addition, PGI(2) or carbaprostacyclin significantly increased the kinase activity of a (p175 kDa) receptor tyrosine kinase and the phosphorylation of extracellular signal-regulated kinase (ERK) 2. Addition of a monoclonal antibody against transforming growth factor (TGF)-alpha, but not insulin-like growth factor-I, to the culture dose-dependently inhibited the PGI(2)- or carbaprostacyclin-induced hepatocyte mitogenesis. Furthermore, treatment with the IP-receptor agonists significantly increased the secretion of TGF-alpha to the culture medium. These results indicate that the IP receptor agonist-induced hepatocyte mitogenesis is mediated by autocrine secretion of TGF-alpha followed by activation of a receptor tyrosine kinase / ERK pathway.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
1347-8613
pubmed:author
pubmed:issnType
Print
pubmed:volume
109
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
618-29
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:19346670-Animals, pubmed-meshheading:19346670-Cell Count, pubmed-meshheading:19346670-Cell Proliferation, pubmed-meshheading:19346670-Cell Separation, pubmed-meshheading:19346670-Cells, Cultured, pubmed-meshheading:19346670-DNA, pubmed-meshheading:19346670-Dose-Response Relationship, Drug, pubmed-meshheading:19346670-Enzyme-Linked Immunosorbent Assay, pubmed-meshheading:19346670-Extracellular Signal-Regulated MAP Kinases, pubmed-meshheading:19346670-Hepatocytes, pubmed-meshheading:19346670-Male, pubmed-meshheading:19346670-Protein-Tyrosine Kinases, pubmed-meshheading:19346670-Rats, pubmed-meshheading:19346670-Rats, Wistar, pubmed-meshheading:19346670-Receptors, Epoprostenol, pubmed-meshheading:19346670-Signal Transduction, pubmed-meshheading:19346670-Transforming Growth Factor alpha
pubmed:year
2009
pubmed:articleTitle
IP receptor agonist-induced DNA synthesis and proliferation in primary cultures of adult rat hepatocytes: the involvement of endogenous transforming growth factor-alpha.
pubmed:affiliation
Department of Clinical Pharmacology, Faculty of Pharmaceutical Sciences, Josai University, Sakado, Japan.
pubmed:publicationType
Journal Article